Papillotome - ANVISA Registration 10368410005

Access comprehensive regulatory information for Papillotome in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10368410005 and manufactured by KOBI MEDIZINTECHNIK GMBH. The registration is held by EUROPA MEDICO SERVICE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MEDI-GLOBE GMBH, OLYMPUS MEDICAL SYSTEMS CORP., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.